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Analysis of IL-29 / IFNL1 / IL29 by ELISA (CAT#: STEM-MB-1550-LGZ)

Introduction

Interleukin-29 (IL-29), also known as interferon λ1(IFN-λ1), is a member of the spiral cytokine family and is a type III interferon. Its amino acid sequence is highly similar to that of another type III interferon, IL-28. The IL-29 gene is found on human chromosome 19, but not in the mouse genome. IL-29 plays an important role in host defense against microorganisms, and its gene is highly upregulated in virus-infected cells. IL-29 has significant antiviral activity and immunomodulatory properties that inhibit viral replication by inducing a cellular antiviral response similar to that activated by IFN-α/β. However, IL-29 binds to a unique receptor, so it may act synergically with IFN-α/β or IFN-γ to inhibit viral replication during natural infection, or in combination with other cytokines to treat chronic viral infections such as hepatitis C (HCV). The antiviral activity of IL-29 includes up-regulation of Class I MHC expression on the cell surface and PKR expression. The ligand/receptor complex appears to conduct signaling through the Jak-STAT pathway.




Principle

Enzyme-linked immunosorbent assay (ELISA) is an enzyme-labeled solid phase immunoassay technique. Its basic principle is to bind the antigen (or antibody) to the solid phase carrier, and the antigen (or antibody) and a certain enzyme link to enzyme labeled antigen (or antibody). During detection, the sample to be tested and the enzymic antigen (or antibody) react with the antigen (or antibody) on the solid phase carrier according to certain procedures, and then remove the unreacted part by washing method. After adding the substrate, the substrate is catalyzed by the enzyme on the solid phase carrier to produce colored substances. Through qualitative or quantitative detection of the amount of colored products, the content of the substance to be measured in the sample can be determined.

Applications

Immunology/Inflammation

Procedure

1. Add standards or samples to each well and incubate.
2. Pour off the liquid in the well, biotinylated antibody working solution and incubate.
3. Add enzyme conjugate working solution and incubate.
4. Add substrate TMB and incubate.
5. Add stop solution and measure OD value.
6. Calculation of results.

Materials

• Sample Type: Serum, plasma, cell culture supernatant and other biological samples
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